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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791889Generated: October 27, 2026

Water → methyl (2S,4R)-4-(2-benzoxazolyl)amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylate

https://huagongshe.com/reaction/1791889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant1-tert-butyl 2-methyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylateHCID 7009918—
SolventTetrahydrofuranHCID 8028—
Productmethyl (2S,4R)-4-(2-benzoxazolyl)amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylateHCID 69754879—

Reaction Steps

Methyl (2S,4R)-4-amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylate [product of Reference Example 4(2), 3.32 g] and triethylamine (1.4 mL) were dissolved in tetrahydrofuran (20 mL). 2-Chlorobenzoxazole (0.86 mL) was added thereto and the mixture was stirred at room temperature for 48 hr. The reaction mixture was added to water and extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogencarbonate solution and brine, and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography to give methyl (2S,4R)-4-(2-benzoxazolyl)amino-1-tert-butoxycarbonylpyrrolidine-2-carboxylate (1.48 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074794B2
Source datasetuspto-grants-2006_07
ORD IDord-12c1e64ab7074546a3d625ad998258d9
Source noteuspto-grants-2006_07